Home › Researcher directory › Imen Chabchoub
Imen Chabchoub
Affiliation : University of Sfax · Hôpital Farhat Hached · Hopital Universitaire Hedi Chaker · Faculty of Medicine of Sfax · University of Sousse
- 139Publications (affiliation in Tunisia)
- 180Total publications
- 1067Citations
- 18h-index
Research profile
Imen Chabchoub has 139 indexed publications (2013–2026). Their work appears mainly in “La Revue de Médecine Interne”, “Archives de Pédiatrie” and “Annals of Oncology”. Their most cited article, “Clinical characteristics and prognosis of traumatic head injury following road traffic accidents admitted in ICU “analysis of 694 cases”” (2017), has been cited 55 times. 23 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Metabolism and Genetic Disorders
- Genomics and Rare Diseases
- Autoimmune and Inflammatory Disorders Research
- Histiocytic Disorders and Treatments
- Autoimmune and Inflammatory Disorders
Publications (139)
- A novel homozygous MICOS13 frameshift mutation causing mitochondrial hepatoencephalopathy and mtDNA depletion: clinical characterization and dynamic structural simulation
- Correlation of epigenetic markers with glioblastoma patients’ survival and molecular subtypes: insights from methylation-specific MLPA analysis
- Pediatric Colorectal Cancer in Africa: A Multicenter Study on Epidemiology, Management, and Outcomes Between 2000 and 2023
- Schwachman Diamond-Like Syndrome Due to a Novel Variant of DNAJC21 Gene: A Case Report and Literature Review
- Primary adrenal insufficiency in children excluding congenital adrenal hyperplasia: insights from 33-year single-center experience in Tunisia
- Study of clinical manifestations and etiologies of megaloblastic anemia in children
- Dihydrolipoamide dehydrogenase deficiency in two unrelated Tunisian children
- Rapid desensitization to insulin in a patient with diabetic ketoacidosis and insulin allergy
- Report of a missense TJP2 variant associated to PFIC4 with a pronounced phenotypic variability: Focus on the structural effects on the protein level
- Présentation pseudo-systémique insolite d’une fièvre Q
- Epidemiological and clinical features of Kawasaki disease and risk factors for cardiac involvement: A study about 32 Tunisian children
- Rare causes of pediatric primary adrenal insufficiency: Data from a large nationwide Tunisian cohort
- Novel combination of TTN and CTNNA3 Pathogenic variant leading to Familial Dilated Cardiomyopathy: From acute heart failure to subclinical phenotypes.
- Activité physique et qualité de vie chez les survivantes du cancer du sein
- Predictive Factors of Cancer Patients' Satisfaction with Quality of Healthcare Services Received at the Middle Euphrates Cancer Center, Al-Najaf Al Ashraf, Iraq
- Scid in Tunisia: Monocentric study of a series of 142 cases
- Aspirine et prévention de la récidive de la maladie veineuse thromboembolique
- L’histiocytose de Rosai Dorfman : à propos de 3 cas
- Une localisation inhabituelle de la sarcoïdose : l’atteinte gastrique
- Le syndrome de néphrite tubulaire et interstitielle et uvéite (TINU syndrome) en milieu de médecine interne
- 365P Pancreatic cancer in young patients under the age of 45 years old: A comparative study with older patients
- 335P Management, outcome and prognostic factors of metastatic pancreatic cancer
- Thromboses veineuses profondes du membre supérieur : analyse de 28 cas
- Complementary and alternative medicine in oncology: knowledge, attitude and practice among Tunisian healthcare workers
- Rosai-Dorfman Disease With Pure and Multifocal Cutaneous Lesions: A Case Report
- Goutte tophacée Sévère : Une observation clinique particulière
- Severe Tophaceous Gout
- Clinical features and outcomes in patients with human immunodeficiency virus-negative, Castleman’s disease: a single medical center study in Tunisia
- PO43 Budd Chiari Syndrome
- Médiastinite fibrosante idiopathique dans le cadre d’une fibrose multifocale révélée par une thrombose veineuse du membre supérieur : à propos d’une observation particulière
- Profil étiologique des thromboses de la veine cave supérieure
- Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys
- Rosai-Dorfman disease with lymph node, bone, and kidney involvement
- Syndrome de Wells bulleux : une observation rare
- Ophthalmic and Genetics Profiles of Cystinosis in Tunisian Patients
- Le ressenti des patients quant à la corticothérapie au long cours au cours du lupus érythémateux systémique
- Thyroïdite d’Hashimoto associée à la sclérodermie systémique
- Molecular Characterization of CNTS Mutations in Tunisian Patients with Ocular Cystinosis
- Adenocarcinoma of intestinal type arising in mature cystic teratoma of ovary: A diagnostic dilemma
- Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations
- Burn-out of the Medical Oncology Health Care Professionals and Associated Factors in Tunisia
- The Current Status of Pancreatic Cancer in Tunisia
- Clinical and serological profile of systemic sclerosis in Tunisia: A retrospective observational study
- Pulmonary embolism in intensive care units: More frequent or more Known? Prospective study of 75 cases
- Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease
- Érythème induré de Bazin : étude anatomoclinique de 8 cas
- La leishmaniose érysipéloïde : étude rétrospective de 28 cas
- Disseminated lymphoblastic lymphoma revealed by an isolated third cranial nerve palsy
- Apport de la dermoscopie dans une ectoparasitose rare : Dermanyssus gallinae
- La pellagre : un diagnostic à ne pas méconnaître
- Forme hypodermique du syndrome de Sweet à type de nouures sous cutanées
- Epidemiology, treatment modalities and prognostic factors of colon cancer in the central region of Tunisia
- Azathioprine : un traitement prometteur des mucinoses
- Granulome sur cicatrice de zona : une rare réaction isotopique de Wolf
- Insensibilité congénitale à la douleur révélée par des ulcérations cutanées
- Les macrochéilites granulomateuses : à travers une série hospitalière de 14 cas
- Nodules cutanés multiples des mains : un cas de réticulo-histiocytose multicentrique
- Pyoderma gangrenosum et lupus érythémateux systémique : une association rare
- A novel TBX1 missense mutation in patients with syndromic congenital heart defects
- Trends and current challenges of breast cancer in Tunisia: a retrospective study of 1262 cases with survival analysis
- Exclusive meningeal relapse of a malignant thymoma after a complete response with neoadjuvant chemotherapy
- Gastric cancer in young patients under the age of 45 years old: A comparative study with older patients
- Prognostic factors for gastric cancer after curative gastrectomy
- Outcome and prognostic factors of gastric cancer in Tunisia
- Maladie de Rendu-Osler et maladie veineuse thromboembolique récidivante
- Clinical characteristics and prognosis of traumatic head injury following road traffic accidents admitted in ICU “analysis of 694 cases”
- Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome
- Severe scorpion envenomation: pathophysiology and the role of inflammation in multiple organ failure
- Pulmonary embolism following severe traumatic brain injury: incidence, risk factors and impact outcome
- Value of troponin levels in the diagnosis of cardiac dysfunction in moderate scorpion envenomation
- Yarrowia lipolytica fungemia in patients with severe polytrauma requiring intensive care admission: analysis of 32 cases
- Transient neonatal diabetes mellitus and activating mutation in the KCNJ11 gene in two siblings
- Particularités de la sclérodermie masculine
- Atteinte digestive au cours de la sclérodermie systémique : une série de 77 cas
- Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome
- Molecular Diagnostic and Prognostic Subtyping of Gliomas in Tunisian Population
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene
- Chylomicron retention disease: A rare cause of chronic diarrhea
- Management of cholestatic pruritus in children with Alagille syndrome: Case report and literature review
- Macrophagic activation syndrome related to an infection by Rickettsia conorii in a child
- Allergie aux protéines du lait de vache : histoire naturelle et facteurs de persistance
- Un syndrome d’activation macrophagique révélant un déficit héréditaire en lipase acide !
- Chediak-Higashi syndrome presenting in accelerated phase
- Comorbidity in the Tunisian population
- Neonatal purulent meningitis in southern Tunisia: Epidemiology, bacteriology, risk factors and prognosis
- Incidence and impact outcome of hyperglycaemia in severe scorpion envenomed children requiring intensive care admission
- Atypical teratoid rhabdoid tumor of the lateral ventricle
- Occipital dermoid cyst associated with dermal sinus complicated with meningitis: A case report
- Miller-Dieker syndrome: A report of a new case and review of the literature
- Typhoid fever complicated with hemophagocytic syndrome in an 11-year-old child
- Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
- Vertebral metastases from intracranial meningioma
- SFP PC-04 - Profil psychologique des enfants atteints de déficit en hormone de croissance : étude de 30 observations
- La maladie de Rendu-Osler-Weber : à propos d’une nouvelle observation pédiatrique
- PO-0043 Classic Infantile-onset Pompe Disease: A Study Of 8 Cases
- Le cancer du sein chez l’homme : similaire ou différent à celui de la femme
- Congenital heart disease in 37,294 births in Tunisia: birth prevalence and mortality rate
- A novel MT-CO2 m.8249G > A pathogenic variation and the MT-TW m.5521G > A mutation in patients with mitochondrial myopathy
- Étude de la sexualité chez les femmes tunisiennes en rémission complète d'un cancer du sein non métastatique, à propos de 100 femmes
Publication venues
- La Revue de Médecine Interne × 18
- Archives de Pédiatrie × 8
- Annals of Oncology × 6
- Annales d Endocrinologie × 3
- Annales de Dermatologie et de Vénéréologie × 3
- Intensive Care Medicine × 3
Publications per year
- 20264
- 20259
- 202410
- 20238
- 20222
- 20215
- 20204
- 201916
- 20187
- 20179
Collaborations
Partner institutions : Hopital Universitaire Habib Bourguiba · Hôpital La Rabta · Hôpital Sahloul · Tunis El Manar University · Institut Pasteur de Tunis
Co-authors
- Mongia Hachicha
- Hajer Aloulou
- Thouraya Kamoun
- Slim Ben Ahmed
- Zouhir Bahloul
- Faten Ezzairi
- Leïla Ben Fatma
- Sana Kmiha
- Ines Maaloul
- Sameh Marzouk
- Imtinene Belaid
- Lamia Sfaihi
Bibliographic data from OpenAlex (open database).
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